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NAME
ID NUMBER
: 4103332001
CLASS
SUBJECT
PART 1
OH- =
H- =
(0.0200)
=
PH = -log 5
OH- =
H- =
= 12.30
(0.0200)
=
OH- =
= 12.24
(0.0200)
=
= 0.01540 M
PH = -log 5.68
OH- =
= 0.01760 M
PH = -log 5.68
H- =
= 0.0200 M
(0.0200)
= 12.18
= 0.01320 M
H- =
PH = -log 7.57
OH- =
H- =
= 12.12
(0.0200)
=
PH = -log 9.009
OH- =
H- =
= 12.04
(0.0200)
=
OH- =
= 11.95
(0.0200)
=
= 0.00909 M
PH = -log 1.111
H- =
= 0.01110 M
= 0.00714 M
PH = -log 1.40056
OH- =
H- =
(0.0200)
=
OH- =
= 11.77
(0.0200)
=
OH- =
= 0.00345 M
PH = -log 2.8985
H- =
= 0.00526 M
PH = -log 1.90114
H- =
= 11.85
= 11.53
(0.0200)
=
PH = -log 2.8985
= 0.00169 M
=
= 11.22
OH- =
H- =
(0.0200)
=
PH = -log 1.1904
OH- =
H- =
= 10.92
(0.0200)
=
OH- =
= 0.00017 M
PH = -log 5.8823
H- =
= 0.00084 M
= 10.22
(0.0200)
=
PH = -log 5
= 0.00004 M
=
= 9.22
PART 2
H20 H+ + OH(x)
(x)
Kw = x2
PART 3
[H+] = (0.100)
= 2 x 10 -5M
[H+] = (0.100)
= 1.7 x 10 -4M
[H+] = (0.100)
= 8.3 x 10 -4M
[H+] = (0.100)
= 8.3 x 10 -4M
[H+] = (0.100)
= 1.64x 10 -3M
[H+] = (0.100)
= 3.23x 10 -3M
[H+] = (0.100)
= 4.76x 10 -3M
[H+] = (0.100)
= 6.25x 10 -3M
[H+] = (0.100)
= 7.69x 10 -3M
[H+] = (0.100)
= 9.09x 10 -3M
The addition
The concentration of
The concentration of
in curve
volume of HBr
excess H+
0.00
0.02000
12.30
1.00
0.01760
12.24
2.00
0.01540
12.18
3.00
0.01320
12.12
4.00
0.01110
12.04
5.00
0.00909
11.95
6.00
0.00714
11,85
7.00
0.00526
11.72
8.00
0.00345
11.53
9.00
0.00169
11.22
9.50
0.00084
10.92
9.90
0.00017
10.22
9.99
0.00002
9.22
10.00
7.00
10.01
0.00002
4.78
10.10
0.00017
3.78
10.50
0.00083
3.08
11.00
0.00164
2.79
12.00
0.00323
2.49
13.00
0.00476
2.32
14.00
0.00625
2.20
15.00
0.00769
2.11
Part I
Part II
Part III
pH
16.00
0.00909
HA H+ + A- (Ka = 10-6.15)
(a-x)
(x)
(x)
= Ka x = 1.19 x 10-4
2.04
PART 2
HA + OH- A- + H2O
Initial
After Titration
(1)
: (
( )
(0)
(0)
( )
PH = pKa + log
= 6.15 +
= 4.87
HA + OH- A- + H2O
Initial
After Titration
(1)
: (
(0)
(0)
(
PH = pKa + log
= 6.15 +
= 5.20
HA + OH- A- + H2O
Initial
After Titration
(1)
: (
(0)
(0)
( )
PH = pKa + log
= 6.15 +
= 5.55
HA + OH- A- + H2O
Initial
After Titration
(1)
: (
( )
(0)
(0)
PH = pKa + log
= 6.15 +
= 5.78
HA + OH- A- + H2O
Initial
After Titration
(1)
: (
(0)
(0)
(
PH = pKa + log
= 6.15 +
= 5.97
HA + OH- A- + H2O
Initial
After Titration
(1)
: (
(0)
(0)
(
PH = pKa + log
= 6.15 +
= 6.15
HA + OH- A- + H2O
Initial
After Titration
(1)
: (
(0)
(0)
(
PH = pKa + log
= 6.15 +
= 6.33
HA + OH- A- + H2O
Initial
After Titration
(1)
: (
(0)
(0)
(
PH = pKa + log
= 6.15 +
= 6.52
HA + OH- A- + H2O
Initial
After Titration
(1)
: (
(0)
(0)
(
PH = pKa + log
= 6.15 +
A
HA
9 00
10
10
10
= 7.10
HA + OH- A- + H2O
Initial
After Titration
:
: (
(1)
05
10
9 50
10
(0)
(0)
(
9 50
10
PH = pKa + log
A
HA
9 50
10
05
10
= 6.15 +
= 7.43
HA + OH- A- + H2O
Initial
After Titration
:
: (
(1)
0 10
10
9 90
10
(0)
(0)
(
9 90
10
PH = pKa + log
= 6.15 +
A
HA
9 90
10
0 10
10
= 8.15
PART 3
A- + H2O HA + OH(a-x)
(x)
(x)
Kb =
HA + OH- A- + H2O
: (1)
(1)
(0)
: (0)
(0)
(1)
Initial
Chemical reaction
[A ] = 0.020
x2
a x
= Kb =
K
Ka
50 0
50 0 10 0
= 0.0167M
= 1.43 x 10 -8 x = 1.54
PH = - log [H ] = - log
- log
1 0 x 10 14
1 54 x 10 5
10 -5 M
= 9.18
PART 4
[OH ] = 0.100
50
50 0 10 10
PH = -log
K
OH
= 1.66 x 10 -4 M
= 10.22
[OH ] = 0.100
50
50 0 10 10
PH = -log
[OH ] = 0.100
K
OH
50 0 10 10
K
OH
50 0 10 10
OH
50 0 10 10
K
OH
= 1.66 x 10 -4 M
= 11.67
50
PH = -log
= 1.66 x 10 -4 M
= 11.50
50
= 1.66 x 10 -4 M
= 11.21
50
PH = -log
[OH ] = 0.100
= 10.91
50 0 10 10
PH = -log
[OH ] = 0.100
OH
50
PH = -log
[OH ] = 0.100
= 1.66 x 10 -4 M
= 1.66 x 10 -4 M
= 11.79
[OH ] = 0.100
50
50 0 10 10
PH = -log
[OH ] = 0.100
K
OH
= 11.88
50
50 0 10 10
PH = -log
K
OH
= 1.66 x 10 -4 M
= 1.66 x 10 -4 M
= 11.95
TABLE
The position
pH
Part I
0.00
3.93
Part II
0.50
4.87
1.00
5.20
2.00
5.55
3.00
5.78
4.00
5.97
5.00
6.15
6.00
6.33
7.00
6.52
8.00
6.75
9.00
7.10
9.50
7.43
9.90
8.15
Part III
10.00
9.18
Part IV
10.10
10.22
10.50
10.91
11.00
11.21
12.00
11.50
13.00
11.67
14.00
11.79
15.00
11.88
16.00
11.95
Kb =
x2
(x)
x2
a x 0 08364 x
1.69 x 10
x2
H2O
x2
0 08364 x
0 1410 x 10
x = 1.18 x x2
BH+ +
(x)
OH-
[OH ] = 1.18 x 10
= 4.93
PH = 14-4.93
= 9.07
PART 2
10 14
1 69 x 10 9
Ka = =
= 0.59 x 10
PH
pKa + log
- log
K
K
+ log
0 50
19 60
=0.025
19 60 0 50
19 60
H
0 97
0 025
-log 0 59 x 10
5.23 + 1.58
+ log 38.80
0.97
= 6.81
10 14
1 69 x 10 9
Ka = =
= 0.59 x 10
PH
pKa + log
- log
K
K
+ log
1 00
19 60
=0.05
19 60 1 00
19 60
0.94
H
0 94
0 05
-log 0 59 x 10
5.23 + 1.27
+ log 18.9
= 6.50
K
10 14
1 69 x 10 9
Ka = =
= 0.59 x 10
pKa + log
2 00
19 60
=0.10
19 60 2 00
19 60
0.89
PH
- log
K
K
+ log
0 89
0 10
-log 0 59 x 10
5.23 + 0.95
+ log 8.9
= 6.18
K
10 14
1 69 x 10 9
Ka = =
= 0.59 x 10
PH
pKa + log
- log
+ log
5.23 + 0.596
5.826
1 69 x 10 9
19 60 0 50
19 60
02
=0.20
0 79
-log 0 59 x 10
10 14
19 60
Ka = =
4 00
= 0.59 x 10
+ log 38.80
0 50
19 60
=0.25
0.79
PH
pKa + log
- log
K
K
19 60 0 25
19 60
0.98
+ log
0 98
0 25
-log 0 59 x 10
5.23 + 0.593
5.823
+ log 3.92
PART 3
BH+
(a-x)
[A-]
Ka
x
(x)
= 0.08364(
=
x2
a x
x2
0 046 x
= 0.52 x 10-3
[H+]
=0.52 x 10-3
PH
H+
(x)
= 3.27
PART 4
[H+]
= (0.1067) (
=1.18 x 10-3 M
PH
[H+]
= (0.1067) (
=2.10 x 10-3 M
PH
[H+]
= (0.1067) (
=3.24 x 10-3 M
PH
[H+]
= (0.1067) (
=4.50 x 10-3 M
= -log 4.50 x 10-3 M
PH
= 2.346
[H+]
= (0.1067) (
=6.66 x10-3 M
= -log6.66 x10-3 M
PH
= 2.17
[H+]
= (0.1067) (
=0.01067M
PH
= -log0.01067M
= 1.9
TABLE
The position
pH
Part I
0.00
9.07
Part II
0.50
6.80
1.00
6.50
2.00
6.18
4.00
5.826
5.00
5.823
Part III
19.60
3.27
Part IV
20.10
2.93
20.50
2.67
21.00
2.5
22.00
2.346
23.00
2.17
25.00
1.9
PART 1
B
BH+
H2O
(0.10-x)
Kb=
OH-
(x)
(x)
OH
By substitution we got
[OH-] = 3.11 x 10-3 M
x
0 10 x
= 3 11 x 10
PH = 11.49
PART 2
PH
PH
pKa2 + log
=
10.0 + log
11.00
pKa2 + log
=
10.0 + log
10.75
H
9
1
H
85
15
PH
PH
PH
PH
PH
pKa2 + log
=
10.0 + log
10.60
pKa2 + log
=
10.0 + log
10.37
pKa2 + log
=
10.0 + log
10.18
pKa2 + log
=
10.0 + log
10.00
pKa2 + log
=
10.0 + log
H
8
2
H
7
3
H
6
4
H
5
5
H
4
6
=
PH
PH
PH
PH
PH
pKa2 + log
=
10.0 + log
9.63
pKa2 + log
=
10.0 + log
9.40
pKa2 + log
=
10.0 + log
9.05
9.82
pKa2 + log
=
10.0 + log
8.72
pKa2 + log
H
3
7
H
2
8
H
1
9
H
05
19 5
10.0 + log
8.00
01
99
PART 3
[H+] =
Where Ka1 and Ka2 are disosiation constant of acid
BH22+.The concentration of BH+ (C) is determined by the
initial concentration of B solution :
C = (0.1 M) (
) = 0.050 M
Wet got..
[H ] =
)(
(
) (
)
= 3.16 x 10-8M
pH = - log 3.16 x 10-8
= 7.50
)(
In this case, pH =
PART 4
pH
= pKa + log
= 5.0 + log
= 6.995
= 7.00
pH
= pKa + log
= 5.0 + log
= 6.278
= 6.28
pH
= pKa + log
= 5.0 + log
= 5.95
pH
= pKa + log
= 5.0 + log
= 5.6
pH
= pKa + log
= 5.0 + log
= 5.37
pH
= pKa + log
= 5.0 + log
= 5.18
pH
= pKa + log
= 5.0 + log
= 5.0
pH
= pKa + log
= 5.0 + log
= 4.82
pH
= pKa + log
= 5.0 + log
= 4.63
pH
= pKa + log
= 5.0 + log
= 4.40
pH
= pKa + log
= 5.0 + log
= 4.05
pH
= pKa + log
= 5.0 + log
= 3.72
PART 5
C = (0.10 M ) (
) = 0.0333 M
BH+ +
H+
(C-x)
(x)
(x)
Ka1 =
= 1.0 x 10-5
x = 5.72 x 10-4
[H+] = 5.72 x 10-4 M
pH = - log 5.72 x 10-4
= 3.24
PART 6
[H+] = (0.10 M) (
pH
) = 3.22 x 10-4
[H+]= (0.10 M) (
pH
) = 6.25 x 10-3
[H+]= (0.10 M) (
pH
) = 9.09 x 10-3
[H+]= (0.10 M) (
pH
) = 1.18 x 10-2
[H+]= (0.10 M) (
pH
) = 1.43 x 10-2 M
Part
pH
Part I
11.49
11.00
1.5
10.75
10.60
10.37
10.18
10.00
9.82
9.63
9.40
9.05
9.5
8.72
9.9
8.00
10
7.50
10.1
7.0
10.5
6.28
11
5.95
12
5.6
13
5.37
Part II
Part III
Part IV
Part V
Part VI
14
5.18
15
5.00
16
4.82
17
4.63
18
4.40
19
4.05
19.5
3.72
20
3.24
21
2.49
22
2.20
23
2.04
24
1.92
25
1.85